Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704644893, Batch Numbers: 18JG09, 18JG26, 18JG34, 18JG37, 18KG18, 18KG23, 18LG02, 18LG22, 19AG09, 19AG21, 19AG37, 19BG04, 19BG07, 19BG21, 19BG40, 19CT49, 19CT71, 19DT33, 19ET22, 19ET28, 19ET54, 19ET60, 19ET72, 19ET77, 19FT24, 19GT59, 19GT65, 19HT35, 19HT66, 19IT25, 19JT22, 19JT29, 20AT53, 20BT23, 20BT27, 20BT47, 20CT12, 20CT36, 20CT51, 20DT09, 20DT37, 20ET16, 20ET28, 20GT06, KME20H2016, KME20J0326, KME20K0155, KME20K0156, KME20K1885, KME20K2582, KME20K3586, KME20L1485, KME20L1836, KME20L1837, KME20L2400, KME20M0812, KME21A1895, KME21A1896, KME21A2805, KME21A2806, KME21B0578, KME21B1677, KME21C0532, KME21C0534, KME21C2645, KME21C3512, KME21C3513, KME21D1023, KME21D1429, KME21J1143, KME21J1407, KME21J1408, KME21L2341, KME21L2342, KME21M0030, KME22B2145, KME22C0914, KME22C1231, KME22C1232, KME22C1823, KME22C2258, KME22C2260, KME22C3451, KME22E1030, KME22F0301, KME22G0908, KME22G0909, KME22H0667, KME22J0698, KME22K0017, KME22K0919, KME22K0920, KME22K3076
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- TELEFLEX LLC
- Reason for Recall:
- Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
Product Codes/Lot Numbers:
UDI/DI 14026704644893, Batch Numbers: 18JG09, 18JG26, 18JG34, 18JG37, 18KG18, 18KG23, 18LG02, 18LG22, 19AG09, 19AG21, 19AG37, 19BG04, 19BG07, 19BG21, 19BG40, 19CT49, 19CT71, 19DT33, 19ET22, 19ET28, 19ET54, 19ET60, 19ET72, 19ET77, 19FT24, 19GT59, 19GT65, 19HT35, 19HT66, 19IT25, 19JT22, 19JT29, 20AT53, 20BT23, 20BT27, 20BT47, 20CT12, 20CT36, 20CT51, 20DT09, 20DT37, 20ET16, 20ET28, 20GT06, KME20H2016, KME20J0326, KME20K0155, KME20K0156, KME20K1885, KME20K2582, KME20K3586, KME20L1485, KME20L1836, KME20L1837, KME20L2400, KME20M0812, KME21A1895, KME21A1896, KME21A2805, KME21A2806, KME21B0578, KME21B1677, KME21C0532, KME21C0534, KME21C2645, KME21C3512, KME21C3513, KME21D1023, KME21D1429, KME21J1143, KME21J1407, KME21J1408, KME21L2341, KME21L2342, KME21M0030, KME22B2145, KME22C0914, KME22C1231, KME22C1232, KME22C1823, KME22C2258, KME22C2260, KME22C3451, KME22E1030, KME22F0301, KME22G0908, KME22G0909, KME22H0667, KME22J0698, KME22K0017, KME22K0919, KME22K0920, KME22K3076
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1839-2023
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